Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

B cell cytopenia in two brothers with hyper-IgD and periodic fever syndrome.

European journal of pediatrics - 1 Jul 2009

Sornsakrin M, Wenner K, Ganschow R

Abstract excerpt

UNLABELLED: We report on two brothers with hyperimmunoglobulinemia D (patient 1: serum immunoglobulin D [IgD] concentration initially 61 IU/ml, later on 340 IU/ml; patient 2: serum IgD concentration 144 IU/ml; normal <100 IU/ml, 97th centile) and periodic fever syndrome (HIDS). Both are compound...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Periodicity
Share to Agammaglobulinemia
Share to Azathioprine

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Immunoglobulin D

Share to Immunoglobulins, Intravenous

Share to Lymphopenia

Share to Mevalonate Kinase Deficiency

Share to Prednisone

Source

Identifiers

PMID: 18839211
DOI: 10.1007/s00431-008-0843-6

Genes

MVK

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18839211-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

B cell cytopenia in two brothers with hyper-IgD and periodic fever syndrome.PMID 18839211Read ↗

A patient with hyper-IgD syndrome responding to anti-TNF treatment.Semantic proximity Read ↗

Hyperimmunoglobulinaemia D syndrome: a rare cause of prolonged fever and treatment with anti-interleukin 1 agent.Semantic proximity Read ↗

Mevalonate kinase deficiency (hyper IgD syndrome with periodic fever)--different faces with separate treatments: two cases and review of the literature.Semantic proximity Read ↗

[Hyperimmunoglobulinemia D and periodic fever syndrome. A phenotypical analysis of a Spanish family].Semantic proximity Read ↗

Hyper-IgD syndrome with novel mutation in a Japanese girl.Semantic proximity Read ↗

[Periodic fever with increased IgD].Semantic proximity Read ↗

Elevated immunoglobulin D levels in children with PFAPA syndrome.Semantic proximity Read ↗

Molecular analysis of MVK mutations and enzymatic activity in hyper-IgD and periodic fever syndrome.Semantic proximity Read ↗

Intermittent neutropenia as an early feature of mild mevalonate kinase deficiency.Semantic proximity Read ↗

Clinical and molecular variability in childhood periodic fever with hyperimmunoglobulinaemia D.Semantic proximity Read ↗

Favorable preliminary experience with etanercept in two patients with the hyperimmunoglobulinemia D and periodic fever syndromeSemantic proximity Read ↗

Molecular analysis of the MVK and TNFRSF1A genes in patients with a clinical presentation typical of the hyperimmunoglobulinemia D with periodic fever syndrome: a low-penetrance TNFRSF1A variant in a heterozygous MVK carrier possibly influences the phenotype of hyperimmunoglobulinemia D with periodic fever syndrome or vice versa.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.